A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5886889



Internal ID22661878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:68553652..68554298hg38UCSC Ensembl
chrX:67773494..67774140hg19UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg38647
hg19647
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17468373
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5886889
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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